scholarly journals The effect of the concentration of alkaline activator and aging time on the structure of metakaolin based geopolymer

2020 ◽  
Vol 52 (2) ◽  
pp. 219-229
Author(s):  
Marija Ivanovic ◽  
Ljiljana Kljajevic ◽  
Jelena Gulicovski ◽  
Marijana Petkovic ◽  
Ivona Jankovic-Castvan ◽  
...  
Keyword(s):  
Aging Time ◽  
Mass Spectra ◽  
Surface Characterization ◽  
Alkali Activation ◽  
X Ray Diffraction ◽  
Structural Reorganization ◽  
X Ray ◽  
Fourier Transformation Infrared Spectroscopy ◽  
Alkaline Activator

This paper outlines the production of an inorganic polymer/geopolymer using a metakaolin by an environmental friendly, energy saving, clean technology to conserve natural environment and resources. The influence of alkali activation, i.e. different concentration of NaOH as a component of alkali activator mixture on the process of geopolymerization of metakaolin is investigated. Also, process of aging time of geopolymer is followed by several analytical methods. The structure of metakaolin and metakaolin based geopolymers and their physicochemical properties were studied using X-ray diffraction (XRD), Fourier transformation infrared spectroscopy (FTIR) and after 28days scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS) was applied for the surface characterization of the samples. A shift of the Si-O or Si-O-X (X=Al, Si, Na...) bands as the molarity of activator increasing during geopolymerization process was observed by FTIR. Mass spectra of geopolymers were characterized by MALDI TOF mass spectrometer. Structural reorganization of geopolymer samples occurs during the curing/aging in accordance with a geopolymerization mechanism.

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

Preparation and Application of Lead Dioxide Electrode for Zinc Electrolysis

2013 ◽  
Vol 785-786 ◽  
pp. 1125-1129
Author(s):  
Xiao Yong Yang ◽  
Pei Xian Zhu ◽  
Yun Sen Si
Keyword(s):  
Surface Characterization ◽  
Catalytic Properties ◽  
Lead Dioxide ◽  
Manufacturing Cost ◽  
X Ray Diffraction ◽  
Simulation Test ◽  
X Ray ◽  
Zinc Smelter ◽  
Lead Dioxide Electrode

According to the process of anodic oxygen evolution in sulfate system for zinc electrolysis,Ti-base lead dioxide electrode can be prepared to use in this case.The surface characterization of the electrode was studied by Scanning electron microscopy(SEM) and X-ray diffraction(XRD).The electrode lifetime was tested in 1mol/L H2SO4solution at 60°C,and the electro-catalytic properties was examined by polarization curves.Then these samples was enlarged and simulation test was conducted at Mengzi marriage zinc smelter in Yunnan.The results show that the electro-catalytic properties is better and the electrodes lifetime is longer compared to the traditional lead electrode.Moreover,it has a significant effect in reducing energy consumption, manufacturing cost and improving the production and grade of zinc.

Surface Characterization of Carbon-Bearing Magnetite (CBM) and Carbon-Bearing Ni(II)-Ferrite (CBNF)

1994 ◽  
Vol 344 ◽  
Author(s):  
T. Sano ◽  
K. Akanuma ◽  
M. Tsuji ◽  
Y. Tamaura
Keyword(s):  
Photoelectron Spectroscopy ◽  
Spinel Structure ◽  
Surface Characterization ◽  
Carbon Deposition ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Oxygen Ions ◽  
Diffraction Patterns

AbstractOxygen-deficient magnetite (ODM; Fe3O4-δ, δ>0) synthesized by reduction of magnetite with H2 at 300°C decomposed CO2 to carbon with an efficiency of nearly 100% at 300°C. In this reaction, two oxygen ions of the CO2 were incorporated into the spinel structure of ODM and carbon was deposited on the surface of ODM with zero valence to form visible particles. The particles of carbon separated from ODM were studied by Raman, energy-dispersive X-ray and wave-dispersive X-ray spectroscopies. The carbon which had been deposited on the ODM was found to be a mixture of graphite and amorphous carbon in at least two levels of crystallization. X-ray photoelectron spectroscopy and X-ray diffraction patterns of the carbon-bearing magnetite (CBM) showed no indication of carbide (Fe3C) or metallic iron (α-Fe) phase formation. In the C 1s XPS spectra of the CBM, no peaks were observed which could be assigned to CO2 or CO. X-ray diffractometry, chemical analysis and TG-MS measurement showed that the carbon-bearing Ni(II)-ferrite (CBNF) (Ni(II)/Fetotal = 0.15) synthesized by the carbon deposition reaction from CO2 with the H2-reduced Ni(II)-ferrite was represented by (Ni0.28Fe2.72O4.00)1-δ (Ni2+06.9Fe2+2.31O3.00)δCτ (δ= 0.27, τ= 0.17). The carbon of the CBNF gave the CIOlayer-like oxide containing some Ni2+ ions.

Synthesis and Characterization of Three Novel Nitrogen-containing Macrolides

2011 ◽  
Vol 66 (9) ◽  
pp. 930-934
Author(s):  
Xin Leng ◽  
Bingqin Yang ◽  
Yuanyuan Liu ◽  
Yi Xie ◽  
Jie Tong
Keyword(s):  
Nmr Spectroscopy ◽  
Hydrogen Bonds ◽  
1H Nmr Spectroscopy ◽  
Mass Spectra ◽  
Synthesis And Characterization ◽  
Stacking Interactions ◽  
X Ray Diffraction ◽  
Preparation Methods ◽  
X Ray

Three novel nitrogen-containing macrolides have been synthesized by esterification. All of them have been characterized by infrared (IR), elemental analysis, mass spectra (MS), and 1H NMR spectroscopy, and their crystal structures were determined by single-crystal X-ray diffraction. The preparation methods and the intermolecular associations based on C-H・・・O hydrogen bonds and π- π stacking interactions are discussed.

Sulphur-selenium compounds

1969 ◽  
Vol 22 (11) ◽  
pp. 2301 ◽  
Author(s):  
CR Ailwood ◽  
PE Fielding
Keyword(s):  
Optical Absorption ◽  
Absorption Edge ◽  
Mass Spectra ◽  
Optical Transition ◽  
Optical Absorption Edge ◽  
X Ray Diffraction ◽  
Selenium Compounds ◽  
X Ray ◽  
Direct Optical Transition

The characterization of various mixtures obtained by fractional recrystallization of sulphur-selenium melts is described. Optical absorption spectra of thin films, mass spectra, and X-ray diffraction data reveal two distinct ranges of homogeneity, the break occurring at 14 at. % Se. The optical absorption edge of crystals containing less than 14 at. % Se varies linearly with composition. A direct optical transition to the conduction band of S8 and a transition due to trapped excitons are thought to contribute to the excessive width of this absorption edge.

Synthesis and Characterization of PMMA/MMT Nanocomposites

2012 ◽  
Vol 182-183 ◽  
pp. 249-253
Author(s):  
Jun Qiao ◽  
Jia Wei Shen ◽  
Xiang Hong Huang ◽  
Qian Feng Zhang
Keyword(s):  
Methyl Methacrylate ◽  
Fourier Transformation ◽  
Raw Materials ◽  
Polymerization Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Fourier Transformation Infrared Spectroscopy ◽  
Thermal Stability Of

PMMA/MMT nanocomposites has been prepared by using methyl methacrylate (MMA), montmorillonite (MMT) and ethanolamine as the raw materials via an in-situ free radical polymerization process. The as-prepared nanocomposites were characterized by Fourier transformation infrared spectroscopy (FTIR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). The results show that the poly(methyl methacrylate) and inorganic montmorillonite have been effectively combined. The structure and thermal stability of the as-prepared nanocomposites are different from the content of MMT in the nanacomposites.

Preparation and characterization of uniform submicrometer metal niobate particles. I. Lead niobate

1991 ◽  
Vol 6 (4) ◽  
pp. 840-850 ◽  
Author(s):  
Myung Jin Kim ◽  
Egon Matijević
Keyword(s):  
Aging Time ◽  
Decomposition Method ◽  
Metal Chelate ◽  
X Ray Diffraction ◽  
Chemical Changes ◽  
X Ray ◽  
Chemical Mechanisms

Colloidal amorphous lead niobate particles of different composition and morphologies were obtained by a metal-chelate decomposition method. The nature of the dispersions depended on the conditions of the preparation of the complexes, pH, aging time, and temperature. The structural and chemical changes of the so prepared powders on calcination were investigated by thermal and x-ray diffraction analyses. Chemical mechanisms of the formation and transformation of the particles are suggested.

scholarly journals Effect of Grinding and Resintering on the Fatigue Limit and Surface Characterization of a Y-TZP Ceramic

2016 ◽  
Vol 27 (4) ◽  
pp. 468-475 ◽  
Author(s):  
Gabriela Scatimburgo Polli ◽  
Gabriel Rodrigues Hatanaka ◽  
Filipe de Oliveira Abi-Rached ◽  
Lígia Antunes Pereira Pinelli ◽  
Márcio de Sousa Góes ◽  
...  
Keyword(s):  
Fatigue Limit ◽  
Surface Characterization ◽  
Monoclinic Phase ◽  
The Other ◽  
X Ray Diffraction ◽  
Staircase Method ◽  
X Ray ◽  
Significant Difference ◽  
Fracture Area

Abstract This study evaluated the effect of grinding protocols and resintering on flexural fatigue limit and surface characterization of LavaTM Y-TZP. Bar-shaped specimens (20×4.0×1.2 mm, n=40; 20×4.0×1.5 mm, n=80) were obtained. Half of the thinner specimens (1.2 mm) constituted the as-sintered group (AS), while the thicker ones (1.5 mm) were ground with diamond burs under irrigation (WG) or not (G). The other half of thinner and half of ground specimens were resintered (1000 ºC, 30 min), forming the groups ASR, WGR and GR. Fatigue limit (500,000 cycles, 10 Hz) was evaluated by staircase method in a 4-point flexural fixture. Data were analyzed by 2-way ANOVA and Tukey's test (α=0.05). Surface topography (n=3) and fracture area (n=3) were evaluated by SEM. X-ray diffraction data (n=1) was analyzed by Rietveld refinement. ANOVA revealed significant differences (p<0.001) for the grinding protocol, resintering and their interaction. Grinding increased the fatigue limit of non-resintered groups. There was no significant difference among the resintered groups. Resintering significantly increased the fatigue limit of the AS group only. Both protocols created evident grooves on zirconia surface. The failures initiated at the tensile side of all specimens. The percentages (wt%) of monoclinic phase were AS (8.6), ASR (1.2), G (1.8), GR (0.0), WG (8.2), WGR (0.0) before, and AS (7.4), ASR (6.5), G (3.2), GR (0.2), WG (4.6), WGR (1.1) after cyclic loading. Grinding increased the fatigue limit of non-resintered Y-TZP and formed evident grooves on its surface. Resintering provided significant increase in the fatigue limit of as-sintered specimens. In general, grinding and resintering decreased or zeroed the monoclinic phase.

Surface Characterization of Chemical-Mechanical Polished GaAs by Inclined Bragg Plane Triple Crystal X-Ray Diffraction

1992 ◽  
Vol 259 ◽  
Author(s):  
Victor S. Wang ◽  
Richard J. Matyi
Keyword(s):  
Structural Damage ◽  
Surface Characterization ◽  
Reciprocal Lattice ◽  
Bragg Condition ◽  
X Ray Diffraction ◽  
Reciprocal Lattice Point ◽  
X Ray ◽  
Unique Capability

ABSTRACTThe incorporation of triple crystal x-ray diffraction (TCD) under conditions of a nearly grazing incident x-ray beam provides a unique capability to characterize surface and subsurface structural damage. The effects of bromine-methanol chemical-mechanical (CM) polishing on the surface quality of GaAs were investigated by inclined Bragg plane triple crystal x-ray diffraction. GaAs samples polished under varying conditions of Br2 concentration, total polish time, polish wheel rotation speed, and force exerted on the samples were analyzed using TCD profiles from inclined (220) planes, with the samples oriented at both the exact Bragg condition, θB, and at deviations from the exact Bragg condition. As the deviation from the 220 reciprocal lattice point was increased, multiple peaks corresponding to both the dynamic and the kinematic components were observed. The peak positions and the relative intensities of the various peaks were used to characterize the effects of the CM polishing variables on the GaAs surfaces.

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